- Author:
	        		
		        		
		        		
			        		Lit Sin Yong
			        		
			        		
			        		
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			        		;
		        		
		        		
		        		
			        		Noorlita Adam
			        		
			        		
			        		
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			        		Author Information
			        		
 - Publication Type:Journal Article
 - Keywords: Pituitary macroadenoma; Primary hypoparathyroidism; Endocrine autoimmunity,
 - MeSH: Hypopituitarism; Autoimmune Hypophysitis; DiGeorge Syndrome
 - From: Journal of the ASEAN Federation of Endocrine Societies 2014;29(1):86-89
 - CountryPhilippines
 - Language:English
 - Abstract: Primary hypoparathyroidism is caused by a group of heterogeneous conditions in which hypocalcemia and hyperphosphatemia occur as a result of deficient parathyroid hormone (PTH) secretion. The most common cause is surgical excision and damage to the parathyroid gland(s). Nonetheless, autoimmune endocrine disorder of primary hypothyroidism has been well-described in polyglandular autoimmune syndromes (PAS).1 Its association with pituitary lesion may be autoimmune lymphocytic hypophysitis as the cause for pituitary disorder. In this report, we encountered a patient with primary hypoparathyroidism who had a non-functioning pituitary tumour. It was confirmed as pituitary adenoma rather than lymphocytic hypophysitis from the histopathological examination. To our knowledge, this is the first reported case of non-functioning pituitary macroadenoma and primary hypoparathyroidism.
 - Full text:121-Article Text-589-1-10-20140531.pdf
 
            
